SRX18044039 Spondias pinnata SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-501 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550574 SAMN20858430 Spondias pinnata WGS GENOMIC PCR BGISEQ-500 SRX18044040 Garcinia xanthochymus SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-502 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550575 SAMN20703220 Garcinia xanthochymus WGS GENOMIC PCR BGISEQ-500 SRX18044041 Cestrum nocturnum SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-511 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550576 SAMN20858450 Cestrum nocturnum WGS GENOMIC PCR BGISEQ-500 SRX18044042 Elaeocarpus serratus SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-503 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550578 SAMN20858453 Elaeocarpus serratus WGS GENOMIC PCR BGISEQ-500 SRX18044043 Chonemorpha eriostylis SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-504 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550577 SAMN31173809 Chonemorpha eriostylis WGS GENOMIC PCR BGISEQ-500 SRX18044044 Machilus cicatricosa SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-505 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550579 SAMN20703208 Machilus cicatricosa WGS GENOMIC PCR BGISEQ-500 SRX18044045 Callistemon citrinus SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-506 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550580 SAMN20858410 Callistemon citrinus WGS GENOMIC PCR BGISEQ-500 SRX18044046 Eugenia aggregata SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-507 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550581 SAMN20858407 Eugenia aggregata WGS GENOMIC PCR BGISEQ-500 SRX18044047 Pouteria viridis SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-508 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550582 SAMN20703180 Pouteria viridis WGS GENOMIC PCR BGISEQ-500 SRX18044048 Manilkara roxburghiana SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-509 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550583 SAMN20703183 Manilkara roxburghiana WGS GENOMIC PCR BGISEQ-500 SRX18044049 Dovyalis abyssinica SRP332833 PRJNA748537 DNA was extracted using either a DNeasy kit (Qiagen, Valencia, California, USA) or with a modified 2 CTAB method (Doyle and Doyle 1987). Genomic DNAs were sheared by nebulization at 30 psi for 70 sec, yielding an average shear size of 500bp as measured by a Bioanalyzer High-Sensitivity Chip (Agilent Technologies, Inc., Santa Clara, California, USA). Constructed paired-end sequencing libraries with insert sizes of 300500 bp with Illumina TruSeq Nano DNA Sample Prep Kit and sequenced using the BGISEQ-510 at the Beijing Genomics Institution (BGI; Shenzhen, China). SRS15550584 SAMN20858418 Dovyalis abyssinica WGS GENOMIC PCR BGISEQ-500